Table 3.
High | Anthracycline/cyclophosphamide combinationa | |
Carmustine | ||
Chlormethine (mechlorethamine) | ||
Cisplatin | ||
Cyclophosphamide ≥1500 mg/m2 | ||
Dacarbazine | ||
Streptozocin | ||
Moderate | Alemtuzumab | |
Arsenic trioxide | Idarubicin | |
Azacitidine | Ifosfamide | |
Bendamustine | Irinotecan | |
Busulfan | Irinotecan peg-liposomal | |
Carboplatinb | Lurbinectedin | |
Clofarabine | Naxitamab | |
Cyclophosphamide <1500 mg/m2 | Oxaliplatin | |
Cytarabine >1000 mg/m2 | Romidepsin | |
Cytarabine/daunorubicin liposomal | Sacituzumab–govitecanc | |
Daunorubicin | Temozolomided | |
Dinutuximab beta | Thiotepae | |
Doxorubicin | Trabectedin | |
Epirubicin | Trastuzumab-deruxtecanc | |
Low | Aflibercept | Ixabepilone |
Amivantamab | Loncastuximab–tesirine | |
Axicabtagene–ciloleucel | Margetuximab | |
Belinostat | Melphalan–flufenamide | |
Blinatumomab | Methotrexate | |
Bortezomib | Mirvetuximab–soravtansine | |
Brentuximab–vedotin | Mitomycin | |
Cabazitaxel | Mitoxantrone | |
Carfilzomib | Moxetumomab–pasudotox | |
Catumaxomab | Necitumumab | |
Cetuximab | Nelarabine | |
Copanlisib | Paclitaxel | |
Cytarabine ≤1000 mg/m2 | Paclitaxel nab-albumin | |
Decitabine | Panitumumab | |
Docetaxel | Pemetrexed | |
Doxorubicin peg-liposomal | Pertuzumab | |
Elotuzumab | Tafasitamab | |
Enfortumab–vedotin | Tagraxofusp | |
Eribulin | Teclistamab | |
Etoposide | Temsirolimus | |
5-Fluorouracil | Tisagenlecleucel | |
Gemcitabine | Tisotumab–vedotin | |
Gemtuzumab–ozogamicin | Topotecan | |
Inotuzumab–ozogamicin | Trastuzumab–emtansine | |
Isatuximab | Vinflunine | |
Minimal | Asparaginase (calaspargase pegol) | |
Atezolizumab | Nivolumab | |
Avelumab | Obinutuzumab | |
Belantamab–mafodotin | Ofatumumab | |
Bevacizumab | Pembrolizumab | |
Bleomycin | Pixantrone | |
Cemiplimab | Polatuzumab–vedotin | |
Cladribine (2-chlorodeoxyadenosine) | Pralatrexate | |
Daratumumab | Ramucirumab | |
Dostarlimab | Rituximab | |
Durvalumab | Trastuzumab | |
Emapalumab | Tremelimumab | |
Fludarabine | Vinblastine | |
Ipilimumab | Vincristine | |
Mosunetuzumab | Vinorelbine |
The combination of an anthracycline and cyclophosphamide in patients with breast cancer is highly emetogenic.
Emetic potential appears to be at the high end of the moderate category.
Emetic potential appears to be at the high end of the moderate category, most closely resembling that of carboplatin.
No direct evidence found for temozolomide intravenous; as all sources indicate a similar safety profile of oral temozolomide, the classification was based on oral temozolomide.
Classification refers to individual evidence from paediatric trials.